Bianchi A B, Navone N M, Conti C J
Department of Carcinogenesis, University of Texas M.D. Anderson Cancer Center, Smithville 78957.
Am J Pathol. 1991 Feb;138(2):279-84.
A polymerase chain reaction-based procedure was used for the detection of DNA length polymorphisms generated by naturally occurring genetic deletions or insertions of known sequence. This method consists of a simple one-step assay that does not require any restriction enzyme analysis or Southern blot hybridization, allowing identification in ethidium bromide-stained gels. The procedure described here was used to detect loss of heterozygosity at various loci, including the Hbb beta-globin gene cluster, in chemically induced mouse skin tumors, using a variety of tissue preparations, including microdissection of formalin-fixed, paraffin-embedded specimens, short-term cultures, and fluorescence-activated cell sorting of epithelial populations. This approach may be useful in detecting tumor-specific reduction to homozygosity at polymorphic chromosomal loci, allowing the mapping of putative tumor-suppressor loci involved in carcinogenesis.
一种基于聚合酶链反应的方法用于检测由自然发生的已知序列的基因缺失或插入所产生的DNA长度多态性。该方法由一个简单的一步检测组成,不需要任何限制性酶切分析或Southern印迹杂交,可在溴化乙锭染色的凝胶中进行鉴定。这里描述的方法用于检测化学诱导的小鼠皮肤肿瘤中包括Hbbβ-珠蛋白基因簇在内的各个位点的杂合性缺失,使用了多种组织制备方法,包括对福尔马林固定、石蜡包埋标本的显微切割、短期培养以及上皮细胞群体的荧光激活细胞分选。这种方法可能有助于检测多态性染色体位点上肿瘤特异性的纯合性降低,从而确定参与致癌过程的假定肿瘤抑制位点。